Effectiveness of Frontal Plane Adaptability in a Novel Foot Prosthesis (NCT06214026)
The Effectiveness of Frontal Plane Adaptability in a Novel Foot Prosthesis for People With Above-Knee Amputations, Bilateral Amputations, or Limited Mobility
๐ฉบ Plain-English Summary (8th-Grade Level)
People with lower extremity amputation (LEA) have persistent problems with balance, falls, residual limb pain, functional mobility, cognitive attention during gait, and satisfaction with participation in daily activities, despite using prostheses. The purpose of this randomized clinical trial is to advance understanding of how dynamic foot design features may help people with LEA This study will include people with above-knee amputations, or with bilateral amputations, or with below-knee amputations and lower levels of mobility. The main study questions/goals are: 1a) To determine if frontal plane adaptation in a foot prosthesis impacts performance, comfort, activities of daily living, and community mobility in the study populations. To answer this question, we will compare a locked and unlocked version of the novel prosthesis. 1b) To determine how the unlocked investigational foot condition compares to the person's usual foot using the outcomes listed above. 2\) To examine the participants' lived experience during community activities. The study will use performance tests, questionnaires, logbooks, and interviews to monitor person-centered outcomes and perceptions of personal functioning during the use of the investigational foot (locked and unlocked) compared to the person's usual foot.
Who can join: Review the eligibility criteria below.
Location: University of South Florida โ Tampa, Florida
Age range: 16 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (3 Sites)
- University of South Florida โ Tampa, Florida
- WillowWood Global โ Mount Sterling, Ohio
- University of Washington โ Seattle, Washington
๐ Contact the Study Coordinator
Phone: (206) 543-6995
Email: msmersh@u.washington.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Amputation
- Development and Usability of an Adjustable Prosthesis for Aquatic Therapy โ Chicago, Illinois
- GaMA Metric to Quantify Functional Importance of Various Upper Limb Prosthetic Devices โ Chicago, Illinois
- Transfemoral Osseointegrated Prosthesis Limb-Load Symmetry Training โ Aurora, Colorado
- Magnetic Bead Tracking System and eOPRA Implant System With Bionic Prosthesis for Transtibial Amputees โ Boston, Massachusetts
- Personalized Mobility Interventions Using Smart Sensor Resources for Lower-Limb Prosthesis Users โ Chicago, Illinois
- Optimizing Prosthetic Prescription to Mitigate the Effects of Perspiration โ Seattle, Washington
Explore by condition: All Amputation clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.